# MicroPort CRM USA, Inc.

- Location (FDA's records): Arlington
- FDA decisions: 7 (1991–2023): 7 original PMA approvals
- Product codes: NVN (2), DXY (1), NIK (1), MRM (1), LWS (1), LWP (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 10 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- P130010: VEGA Steroid-Eluting Endocardial Leads (VEGA™ R45, VEGA™ R52, and VEGA™ R58) (May 17, 2023)
- P060027: Ovatio CRT System (May 15, 2008)
- P020030: Stelid II/Stelix/Stelix II Endocardial Pacing Lead (Jun 17, 2004)
- P980049: Defender II Model 9201 Implantable Cardioverter Defibrillator (Sep 15, 1999)
- P970024: Angeion Sentinel Implantable Cardioverter Defibrillator (Icd)System and the Angeflex TM Defibrillation Lead System. (Aug 19, 1998)
- P950029: Chorus RM Model 7034 DDDR Pacemaker Incl. Opus RM Model 4534 Ssir Pacemaker (Mar 10, 1997)
- P900022: Chorus DDD Pacemaker (Sep 6, 1991)

Source page: https://510kreport.com/company/microport-crm-usa